Canonical Allele Identifier: PA916010904
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186416
ClinVar RCV Id: RCV000166008 RCV000679237 RCV001085290 RCV001264551 RCV003995471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe11Leu
CA012766
NM_001281492.2:c.33C>G
CA346734518
NM_001281492.2:c.31T>C
CA346734523
NM_001281492.2:c.33C>A